Related Experiment Video
Updated: May 16, 2026

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults
Published on: February 28, 2025
Juvenile cystic adenomyoma
Maryjo Marques Branquinho1, Andreia Leitão Marques, Helena Barros Leite
1Department of Obstetrics and Gynecology, Bissaya Barreto Maternity Hospital, Coimbra, Portugal.
This case study describes juvenile cystic adenomyoma, a rare uterine condition in a teenage girl with severe menstrual pain. Magnetic Resonance Imaging (MRI) was crucial for diagnosing this challenging case.
Area of Science:
- Gynecology
- Pediatric and Adolescent Gynecology
- Diagnostic Imaging
Background:
- Juvenile cystic adenomyoma is a rare benign uterine condition.
- It often presents with severe, intractable dysmenorrhea in young nulliparous women.
- Diagnosis can be challenging due to its rarity and overlapping symptoms with other conditions.
Observation:
- A 17-year-old female experienced progressively worsening dysmenorrhea unresponsive to NSAIDs.
- Magnetic Resonance Imaging (MRI) revealed a cystic uterine lesion.
- The lesion's characteristics, including signal intensity similar to the endometrium and response to hormone suppression, were key diagnostic indicators.
Findings:
- The case confirms juvenile cystic adenomyoma as a cause of severe dysmenorrhea in adolescents.
- MRI demonstrated characteristic features aiding in the definitive diagnosis.
- The cyclic nature of symptoms and MRI findings strongly supported the diagnosis.
Implications:
- This case underscores the importance of advanced imaging like MRI in diagnosing rare gynecological conditions in adolescents.
- Early and accurate diagnosis is crucial for appropriate management and treatment planning.
- Understanding the MRI characteristics of juvenile cystic adenomyoma can improve diagnostic accuracy and patient outcomes.
Related Concept Videos
Urologic Endoscopic Procedure: Cystoscopic Examination
Imaging Studies VI: Voiding Cystourethrography and Cystography
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Appendicitis
Cholecystitis
Appendicitis-II: Diagnostic Studies and Management
Diagnosing Appendicitis
It requires a multifaceted approach, starting with a detailed physical examination to pinpoint the location and nature of the pain and identify any associated symptoms. Laboratory tests play a crucial role. A complete Blood Count (CBC) typically reveals leukocytosis (an increased number of...
